198336-00-4Relevant articles and documents
A convergent approach to the marine natural product eleutherobin: Synthesis of key intermediates and attempts to produce the basic skeleton
Scalabrino, Gaia,Sun, Xiao-Wen,Mann, John,Baron, Anne
, p. 318 - 327 (2007/10/03)
Synthesis of (1R,5R,6R)-2-(6-hydroxymethyl-5-isopropyl-2-methylcyclohex-2-enyl)-N-methoxy-N-m ethylacetamide 8 from R-(-)-phellandrene in six steps, and (3aR*,4S*,6R*,6aS*)-(6-hydroxymethyl-4-methoxy-2,2,6-tri methyl-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl)acetic acid methyl ester 17 from tetrabromoacetone and 2-methoxy-5-methyl-furan in six steps, provided two key fragments which have been combined to produce intermediates for attempted construction of the basic skeleton of eleutherobin.
Synthesis of the tricyclic core of eleutherobin and sarcodictyins and total synthesis of sarcodictyin A
Nicolau,Xu,Kim,Ohshima,Hosokawa,Pfefferkorn
, p. 11353 - 11354 (2007/10/03)
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